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A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects

HIV progression is characterized by immune activation and microbial translocation. One factor that may be contributing to HIV progression could be a dysbiotic microbiome. We therefore hypothesized that the GI mucosal microbiome is altered in HIV patients and this alteration correlates with immune ac...

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Autores principales: Mutlu, Ece A., Keshavarzian, Ali, Losurdo, John, Swanson, Garth, Siewe, Basile, Forsyth, Christopher, French, Audrey, DeMarais, Patricia, Sun, Yan, Koenig, Lars, Cox, Stephen, Engen, Phillip, Chakradeo, Prachi, Abbasi, Rawan, Gorenz, Annika, Burns, Charles, Landay, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930561/
https://www.ncbi.nlm.nih.gov/pubmed/24586144
http://dx.doi.org/10.1371/journal.ppat.1003829
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author Mutlu, Ece A.
Keshavarzian, Ali
Losurdo, John
Swanson, Garth
Siewe, Basile
Forsyth, Christopher
French, Audrey
DeMarais, Patricia
Sun, Yan
Koenig, Lars
Cox, Stephen
Engen, Phillip
Chakradeo, Prachi
Abbasi, Rawan
Gorenz, Annika
Burns, Charles
Landay, Alan
author_facet Mutlu, Ece A.
Keshavarzian, Ali
Losurdo, John
Swanson, Garth
Siewe, Basile
Forsyth, Christopher
French, Audrey
DeMarais, Patricia
Sun, Yan
Koenig, Lars
Cox, Stephen
Engen, Phillip
Chakradeo, Prachi
Abbasi, Rawan
Gorenz, Annika
Burns, Charles
Landay, Alan
author_sort Mutlu, Ece A.
collection PubMed
description HIV progression is characterized by immune activation and microbial translocation. One factor that may be contributing to HIV progression could be a dysbiotic microbiome. We therefore hypothesized that the GI mucosal microbiome is altered in HIV patients and this alteration correlates with immune activation in HIV. 121 specimens were collected from 21 HIV positive and 22 control human subjects during colonoscopy. The composition of the lower gastrointestinal tract mucosal and luminal bacterial microbiome was characterized using 16S rDNA pyrosequencing and was correlated to clinical parameters as well as immune activation and circulating bacterial products in HIV patients on ART. The composition of the HIV microbiome was significantly different than that of controls; it was less diverse in the right colon and terminal ileum, and was characterized by loss of bacterial taxa that are typically considered commensals. In HIV samples, there was a gain of some pathogenic bacterial taxa. This is the first report characterizing the terminal ileal and colonic mucosal microbiome in HIV patients with next generation sequencing. Limitations include use of HIV-infected subjects on HAART therapy.
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spelling pubmed-39305612014-02-25 A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects Mutlu, Ece A. Keshavarzian, Ali Losurdo, John Swanson, Garth Siewe, Basile Forsyth, Christopher French, Audrey DeMarais, Patricia Sun, Yan Koenig, Lars Cox, Stephen Engen, Phillip Chakradeo, Prachi Abbasi, Rawan Gorenz, Annika Burns, Charles Landay, Alan PLoS Pathog Research Article HIV progression is characterized by immune activation and microbial translocation. One factor that may be contributing to HIV progression could be a dysbiotic microbiome. We therefore hypothesized that the GI mucosal microbiome is altered in HIV patients and this alteration correlates with immune activation in HIV. 121 specimens were collected from 21 HIV positive and 22 control human subjects during colonoscopy. The composition of the lower gastrointestinal tract mucosal and luminal bacterial microbiome was characterized using 16S rDNA pyrosequencing and was correlated to clinical parameters as well as immune activation and circulating bacterial products in HIV patients on ART. The composition of the HIV microbiome was significantly different than that of controls; it was less diverse in the right colon and terminal ileum, and was characterized by loss of bacterial taxa that are typically considered commensals. In HIV samples, there was a gain of some pathogenic bacterial taxa. This is the first report characterizing the terminal ileal and colonic mucosal microbiome in HIV patients with next generation sequencing. Limitations include use of HIV-infected subjects on HAART therapy. Public Library of Science 2014-02-20 /pmc/articles/PMC3930561/ /pubmed/24586144 http://dx.doi.org/10.1371/journal.ppat.1003829 Text en © 2014 Mutlu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mutlu, Ece A.
Keshavarzian, Ali
Losurdo, John
Swanson, Garth
Siewe, Basile
Forsyth, Christopher
French, Audrey
DeMarais, Patricia
Sun, Yan
Koenig, Lars
Cox, Stephen
Engen, Phillip
Chakradeo, Prachi
Abbasi, Rawan
Gorenz, Annika
Burns, Charles
Landay, Alan
A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
title A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
title_full A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
title_fullStr A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
title_full_unstemmed A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
title_short A Compositional Look at the Human Gastrointestinal Microbiome and Immune Activation Parameters in HIV Infected Subjects
title_sort compositional look at the human gastrointestinal microbiome and immune activation parameters in hiv infected subjects
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3930561/
https://www.ncbi.nlm.nih.gov/pubmed/24586144
http://dx.doi.org/10.1371/journal.ppat.1003829
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